Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus

Background & objectives: RNA viruses are complex pathogens in terms of their genetic makeup, mutation frequency, and transmission modes. They contain the RNA helicase enzyme, which plays a crucial role in the viral genome replication process. This work aims to develop and screen a potential mole...

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Main Authors: Raghunath Satpathy, Sonali Acharya, Rashmiranjan Behera
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-11-01
Series:Journal of Vector Borne Diseases
Subjects:
Online Access:https://journals.lww.com/10.4103/JVBD.jvbd_188_23
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author Raghunath Satpathy
Sonali Acharya
Rashmiranjan Behera
author_facet Raghunath Satpathy
Sonali Acharya
Rashmiranjan Behera
author_sort Raghunath Satpathy
collection DOAJ
description Background & objectives: RNA viruses are complex pathogens in terms of their genetic makeup, mutation frequency, and transmission modes. They contain the RNA helicase enzyme, which plays a crucial role in the viral genome replication process. This work aims to develop and screen a potential molecule that could function as a dengue virus (DENV) RNA helicase inhibitor. Methods: The present study was performed by taking 26 potential derivatives of gedunin phytochemicals from the PubChem database as ligands. The binding of the compounds was analyzed by in silico docking considering DENV RNA helicase enzyme as the receptor. Results: After a thorough analysis of the docking scores, toxicity, and physicochemical properties, the compound tetrahydrogedunin was obtained as the best. Based on tetrahydrogedunin molecular structure, 100 drug-like molecules were designed using the Data Warrior tool. After screening for drug-likeness and ADMET properties, derivative number 42 was considered as promising. Further comparative docking of derivative 42 and a standard inhibitor molecule ST-610 with DENV RNA helicase enzyme showed binding affinity of 10.0 kcal/mol and -9.6 kcal/mol, respectively. The favorable interaction between DENV RNA helicase and derivative 42 was further validated by 50 nanoseconds molecular dynamics simulation and MM-GBSA analysis. Interpretation & conclusion: Since the antiviral activity of derivative 42 has not been reported till date, the compound was predicted as a novel therapeutic molecule that can act against the dengue virus (DENV) RNA helicase enzyme.
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spelling doaj-art-efda1a2b06be4e83ab23bc5dd95bffb42025-08-20T02:20:55ZengWolters Kluwer Medknow PublicationsJournal of Vector Borne Diseases0972-90622024-11-0161453654610.4103/JVBD.jvbd_188_23Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virusRaghunath SatpathySonali AcharyaRashmiranjan BeheraBackground & objectives: RNA viruses are complex pathogens in terms of their genetic makeup, mutation frequency, and transmission modes. They contain the RNA helicase enzyme, which plays a crucial role in the viral genome replication process. This work aims to develop and screen a potential molecule that could function as a dengue virus (DENV) RNA helicase inhibitor. Methods: The present study was performed by taking 26 potential derivatives of gedunin phytochemicals from the PubChem database as ligands. The binding of the compounds was analyzed by in silico docking considering DENV RNA helicase enzyme as the receptor. Results: After a thorough analysis of the docking scores, toxicity, and physicochemical properties, the compound tetrahydrogedunin was obtained as the best. Based on tetrahydrogedunin molecular structure, 100 drug-like molecules were designed using the Data Warrior tool. After screening for drug-likeness and ADMET properties, derivative number 42 was considered as promising. Further comparative docking of derivative 42 and a standard inhibitor molecule ST-610 with DENV RNA helicase enzyme showed binding affinity of 10.0 kcal/mol and -9.6 kcal/mol, respectively. The favorable interaction between DENV RNA helicase and derivative 42 was further validated by 50 nanoseconds molecular dynamics simulation and MM-GBSA analysis. Interpretation & conclusion: Since the antiviral activity of derivative 42 has not been reported till date, the compound was predicted as a novel therapeutic molecule that can act against the dengue virus (DENV) RNA helicase enzyme.https://journals.lww.com/10.4103/JVBD.jvbd_188_23pathogenic virusesrna helicasemolecular dockingmolecular dynamics simulationdengue virus
spellingShingle Raghunath Satpathy
Sonali Acharya
Rashmiranjan Behera
Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
Journal of Vector Borne Diseases
pathogenic viruses
rna helicase
molecular docking
molecular dynamics simulation
dengue virus
title Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
title_full Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
title_fullStr Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
title_full_unstemmed Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
title_short Computational design, docking, and molecular dynamics simulation study of RNA helicase inhibitors of dengue virus
title_sort computational design docking and molecular dynamics simulation study of rna helicase inhibitors of dengue virus
topic pathogenic viruses
rna helicase
molecular docking
molecular dynamics simulation
dengue virus
url https://journals.lww.com/10.4103/JVBD.jvbd_188_23
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AT sonaliacharya computationaldesigndockingandmoleculardynamicssimulationstudyofrnahelicaseinhibitorsofdenguevirus
AT rashmiranjanbehera computationaldesigndockingandmoleculardynamicssimulationstudyofrnahelicaseinhibitorsofdenguevirus